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In this work the genetic variability of the common shrew populations Sorex araneus L. in Eastern Europe was studied via sequencing of the mitochondrial gene cyt b. A total of 82 sequences of the mitochondrial gene cyt b with a length of 953 basepairs were analyzed, including five chromosome races in a continuous area of the species in forest zone and two races in fragmented area in the steppe zone. Phylogeographic subdivision of the common shrew was not expressed, and there was no significant correlation between genetic and geographic distances in continuous areas. We did not acquire convincing evidence of the influence of narrow hybrid zones between chromosome races on the flow of neutral alleles. A significant p-distance (0.69 ± 0.27%) of geographically close populations of the chromosome race Neroosa indicates the formation of the karyotype of this race in the Pliocene or Pleistocene. In our work, the phylogeographic structure was determined more by species area fragmentation than by its karyotypic features.

The contact points of four karyotypic races (St. Petersburg, Moscow, Seliger and West Dvina) of the common shrew Sorex araneus L. were studied at the Valdai Hills (European Russia) in an area unimpeded by geographic barriers. The populations of the races are separated by narrow hybrid zones that represent the most complex heterozygous hybrid karyotypes. At these points of contact, the morphometric differentiation of karyotype races was examined in 12 cranial measurements in 190 shrews of a known karyotype. A. comparison of the mean values in studied samples of immature shrews revealed statistically significant differences and the correlation of some measurements in order to describe the level of musculus temporalis. It has been proposed that morphometric differences in the karyotypic races were preserved and accumulated because of a 50% reduction of the frequencies of hybrids. The deviation from the Hardy-Weinberg ration in the frequencies of the genotype and haploid sets of chromosomes in the hybrid zones can be attributed to a number of fatalities of hybrid embryos or the nonrandom mating of karyotypic races. The ethological isolation might arise in the evolution of some karyotypic races from the reduced fitness of the hybrids.

The contact zone between Moscow and Western Dvina chromosomal races of common shrew Sorex araneus L. at the south of the Valdai Hights was traced over a distance of 20 km. Within this, close to parapatric, contact zone of chromosomal races the width of sympatry zone was about 500 m (the narrowest among currently known hybrid zones), and the proportion of hybrids was 24.3%. It was shown that in bimodal hybrid zones between chromosomal races of common shrew the width of sympatry zones varied from 0.5 to 13 km. This width does not correlate with the cytogenetic features of the hybrids, and seems to be determined by competitive relations between the races. The hybrid proportion is determined by the type of hybrid heterozygosity, and decreased in the race sympatry zone from 33-40 to 21.5-25.2%. The decrease of the hybrid proportion can be associated with the abnormal fertility of either the first generation, or the backcross hybrids.

Using the data of karyological analysis, the phylogenetic relationships of Caucasian shrew Sorex satunini and the cryptic species of superspecies Sorer araneus were examined. In the population of Sorex satunini from the plain of North Ciscaucasia two deeply radiated cytochrome b genes (A and B) were identified. Genetic distance between haplotype A and B groups constituted 0.0675 +/- 0.008, which is higher than any distance in superspecies S. araneus. Possible introgression of type B haplotypes from the populations of the evolutionary lineage S. subaraneus--S. araneus in Pleistocene and the time of the appearance of the chromosomal polymorphism of S. araneus is discussed. Our results show that the use of only one mitochondrial marker can lead to false conclusions on taxonomic diversity

The work attempts to explain the previously discovered phenomenon of excessive taxonomic status of the species and subspecies of Cuban hutias relative to their protein genetic divergence. The reasons underlying the fragmentary distribution of the species belonging to the family Capromyidae over the Antilles and Bahamas is also considered. Samples of four geographically distant hutia (genera Capromys and Mysateles) populations inhabiting different biotypes were assessed according to 32 allozyme loci. It has been demonstrated that the interpopulation and subspecies differentiation in the gene frequencies in these genera is very low. As for the pattern of polymorphism (Shannon?s measure), the populations and subspecies within these genera are well differentiated and adequate to their morphological differentiation. This suggests that the genetic divergence pattern of hutias in post-Pleistocene was predominantly determined by selection on the background of a relatively rapid formation of multiple morphotypes. It is assumed that the evolution within the family Capromyidae in the earlier and the later periods was associated with the geomorphological and climatic events in the history of the Earth. This standpoint provides for explaining the phenomena of both the excessive taxonomic status of the Cuban Capromyinae and the fragmentary distribution of these species over the Antilles and Bahamas, amazing at a first glance.

In this review, we discuss the processes of fixation of Robertsonian chromosome fusions in populations of the common shrew Sorex araneus L. Various Robertsonian fusions, accumulating in populations, create an illusion of large chromosomal rearrangements, reciprocal translocations of complete chromosome arms. The use of these rearrangements for phylogenetic reconstructions results in false conclusions. Robertsonian fusions accumulate in populations at such stages of the species evolution, when large open or subdivided populations prevail (populations of warm periods of Pleistocene and many present-day populations) and are fixed in small isolated populations and glacial refugia. The formation of monomorphic chromosome races requires a long time, several glaciation epochs during the whole Pleistocene.

To specify the taxonomic rank of form ciscaucasoides (independent species Sylvaemus ciscaucasoides, or intraspecific form of pygmy wood mouse, S. uralensis), a 402-bp the mtDNA cytochrome b gene fragment (402 bp) was examined in S. ciscaucasoides individuals from six geographic localities of the Caucasus and Ciscaucasus, (Krasnodar krai and Adygeya Republic) and 17 S. uralensis individuals from seven localities of the Russian Plai (Saratov oblast, Smolensk oblast, Voronezh oblast, Tula oblast, Moscow oblast, and Tver' oblast). For comparison, the cytochrome b gene was partly sequenced in the samples of yellow necked, S. flavicollis (n = 2, Samara oblast), and Caucasian, S. ponticus (n = 6, Krasnodar krai), wood mice. One Mus musculus specimen from Western Europe, whose nucleotide sequences were deposed in the GenBank, was used as intergeneric outgroup. Phylogenetic trees for the forms examined were constructed based on the mtDNA sequence variation and using the neighbor joining and maximum parsimony methods. The network of the cytochrome b haplotypes was also constructed. The level of genetic divergence was evaluated using Kimura's two-parameter algorithm. Based on the data on the sequence variation in a 402-bp mtDNA cytochrome b gene fragment, the hypothesis on the species status of the ciscaucasicus form was. The mean intergroup distances (d) between the geographic groups of S. uralensis varied from 0.0036 to 0.0152. At the same time, the distances between the pygmy wood mice and the group of S.flavicollis-S. ponticus varies in the range from 0.0860 to 0.0935, and the level of intergeneric genetic differentiation (Sylvaemus-Mus) is higher than the latter index (d = 0.142). Ciscaucasoides should be considered as geographic substitution form of S. uralensis. Furthermore, the Caucasian populations of S. uralensis (= ciscaucasoides) were characterized by a threefold lower value of intergroup genetic divergence (d = 0.0062) than the East European populations (d= 0.0179). This finding pointed to some isolation of Caucasian populations of pygmy wood mouse and depletion of their gene pool. However other molecular genetic data (similarity of nucleotide composition and consistence of the levels of intra- and intergroup distances) suggest the absence of geographic subdivision between Caucasian and East European populations ofS. uralensis relative to the molecular marker examined.

The current condition of the megapopulation of the Przhevalsky horse was assessed using genetic indices of biological diversity of species and genealogical analysis and taking into account both nuclear and non-nuclear (mitochondrial), maternally inherited components of hereditary information.

The variability of the genomes of ten vole species was analyzed by means of taxonomic DNA fingerprinting and polymerase chain reaction using random primers (RAPD-PCR). The dendrograms of genetic similarity between the representatives of the tribe Arvicolinae (Gray, 1821) were constructed, based on the data obtained by means of both methods. The topology of the genetic similarity dendrogram that is based on the RAPD-PCR data generally correlates with the genetic distances estimated from biochemical and karyological data. The results did not confirm the genus status of Terricola. On the other hand, the data from taxonprint analysis suggest the recognition of Lasiopodomys as a separate genus.

Allozyme variation in nine populations of the house mouse Mus musculus L. s. str. was examined. Twenty-five out of 34 analyzed loci were shown to be polymorphic. Estimates of genetic variation were obtained for separate populations and for population groups classified according to their habitat. Populations from Moldova and Tadzhikistan displayed the lowest and highest amounts of allozyme variation, respectively. Variation in town populations was significantly greater than in rural ones. This can be explained by active human-induced migration of mice into towns. All Central Asian populations showed high levels of genic diversity, which is presumably related to their proximity to ancient centers of mice expansion. Allelic distributions in the populations were analyzed.

Electrophoretic methods were used to study protein products of 32 gene loci in the blood of European and Canadian beavers held in captivity at the Voronezh State Nature Reserve. In the studied samples, the levels of polymorphism and average heterozygosity exceeded the average values of corresponding indices determined for beavers that inhabit temperate zones. To what extent the studied samples represent the state of the gene pool of parental populations is discussed. A comparison between allozyme spectra of samples of European and Canadian beavers revealed many coinciding polymorphic loci, on the one hand, and pronounced genetic divergence of these species, on the other.

The electron microscopic analysis of synaptonemal complexes of the Robertsonian translocation heterozygotes (Rb/T) and heterozygotes of the reciprocal translocation (Rb(8, 17)/T(16, 17) 43H revealed three types of translocation configurations (TC). The observed TC were subdivided into three types according to the manner of synapsis: 1) full synapsis of homologues forming trivalent with interstitial centromere in 15%; 2) the centromeric asynapsis (8 and 17-16 chromosomes forming trivalent with the extension region of asynapsis and breakpoint of the reciprocal translocation on chromosome 17 in 70%; 3) centromeric asynapsis (only single chromosome 17-16 of trivalent, when the break point of reciprocal translocation and the absence of centromeric asynapsis of another chromosome 8 formed trivalent in 15%). The frequency of association between trivalents and the XY bivalents is 20% and close proximity is 15% for heterozygotes Rb/T. Which are fertile, while in the sterile heterozygotes Rb(8, 17)/T(16, 17) 43H it is 45% for association and 15% close proximity (total 60%). These data show the significant differences in the contact of translocation configurations with the XY bivalents of fertile heterozygotes, in comparison with the sterile. Thus, it is shown that the chromosome pairing of fertile and sterile mice is clearly distinguished.

Complementation for viability of the compounds tx/ty in complete lethal haplotypes t6, t12, tw5, tw12, tw18, tw73, twPa-1 belonging to the seven basic complementation groups was studied. In the overwhelming majority of crosses a lack of tx/ty offspring was revealed but there is also evidence of non-complete complementation of the tx/ty haplotypes, except for T/tw73XT/tw12, T/tw18XT/t12, T/tw73XT/tw18 crosses in which the level of complementation for viability exceeds 100%. The maternal effect for compound variability was significantly revealed in 9 out of the 19 matings. In addition, reciprocal matings of heterozygotes T/txXT/ty were tested for fertility. In two cases, the maternal effect was also revealed for this character. Comparison of data on viability of the compounds and the fertility of the original strains gives grounds to believe that the tx/ty haplotypes are not completely recessive and partially manifest themselves in the heterozygotes, decreasing fertility in a number of matings. In some cases, these t-haplotypes yield an effect, close to negative complementation, which may be associated with the interaction of the proteins of t-haplotypes.

Fertility of 47 mouse males carrying various combinations of lethal, t-haplotypes (t6/tw18, t12/tw18, Tw73/tw12, tw5/tw18, t6/dt5, t12/tw12, tw5/twPa-1, tw18/twPa-1, tw5/tw12) was studied in crosses with females of different genotypes. The t-haplotypes studied belong to 7 main groups of complementation. The presence of at least two factors of fertility in the t-complex was revealed. The influence of female genotype on the degree of male fertility was also demonstrated. The data presented confirm that different combinations of lethal complete t-haplotypes exhibit sterility, with the exception of t8/tw18 compound.